Over -the -counter cold medicine recalled after a dangerous mixture of products, the FDA warns
Officials say that the accident could lead to "serious adverse events".
Make a cold is never fun, but at least over -the -counter medicine (OTC) can help relief . This is why many people appear at the pharmacy during the first sign of sniffing, sore throat or a cough to collect their brand of choice and to reduce their symptoms. But before you reach your next dose, you may want to check what's in your wardrobe. Indeed, the Food & Drug Administration (FDA) has just announced that a free -free cold drug was recalled after a dangerous mixture of products. Read the rest for more information and to see if you are assigned by the move.
Read this then: Lay Crustry remembered health problems, the FDA warns .
The FDA has just announced a reminder for a medicine against the over -the -counter cold.
It may be time to check the cold drugs you have on hand. On May 19, the FDA announced that Novis Pr LLC had published a voluntary reminder of his pediatric drops DX G-SUPRESS. AE0FCC31AE342FD3A1346EBB1F342FCB
The over -the -counter medication is sold as a "cough decongestionary, expectorant and nasal used for the temporary relief of the symptoms of the common cold" packaged in bottles of 1 ounce inside a box of cardboard. The company claims that the recall affects lot D20911 with the expiration date "10/25" stamped on the packaging.
A mixture of products has created a potentially dangerous situation for consumers.
Depending on the reminder notice, the company withdrew the article from the shelves after discovering that some boxes contained a different product. More specifically, the packaging contains a half-only bottles of an oral anesthetic / analgesic used for "temporary relief for the mouth and gums" instead of children's cold medicine.
The product mixture creates a potentially dangerous situation because the anesthetic / analgesic product contains 60% ethyl alcohol and 5% benzocaine. Society claims that this could cause "serious undesirable events", including alcohol toxicity.
"Infants and young children are subject to deep comoglycemia on a coma, and the ingestion hypothermia of relatively small quantities of ethanol, and deaths have been reported," warns the opinion. Benzocaine could also cause methemoglobinemia, a "condition in which too little oxygen is issued to your cells which can be fatal".
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Here is what you need to do if you have the article assigned in your pharmacy cabinet.
Until now, NOVIS says that he has not received any report of adverse reactions or injuries related to the use of the product. But the company advises customers to the cold drugs recalled to stop using it immediately and return to its place of purchase.
The company adds that it reaches out to distributors and customers by telephone to alert them to the recall. In addition, any person with questions or concerns can contact the company by calling a customer service number listed in the FDA notice. Customers who believe they have experienced health problems or negative effects related to taking the item must immediately contact their health care provider.
Other recent reminders have been published for over -the -counter medicines.
It is not the only time recently that on -the -counter medicines have been removed from the shelves for safety problems. On May 18, the US Consumer Product Safety Commission (CPSC) announced that ACME United had recalled four of his Brand of medicine Allergy and cold medicines. In this case, the company said that the products were not sold in children's resistant packaging, "pose a risk of poisoning if the content is swallowed by young children".
Another recall was issued for seven on -the -counter ADVIL products different sold to Family dollar Earlier this month. In a notice of May 4, the FDA said that 73 lots Medicines were removed from the shelves after the retailer stored the items "apart from the labeled temperature requirements". Customers were invited to make the products assigned to their purchasing store for a full refund.
And on April 26, the FDA announced that the Illinois Akorn Operation Company LLC had published a voluntary reminder for more than 80 of his drugs, including over -the -counter medicines, prescription drugs and pets for pets. The manufacturer pulled market items - which included current products such as artificial tears, an ointment in lidocaine and vitamin D cuts - just more than two months after having deposited for Chapter 7 Bankruptcy And has dismissed all of its employees in its national national production sites.
The company said that without its internal quality insurance program in place, it would no longer be able to support or guarantee that the items will respect the specifications thanks to the rest of their shelf life. Consequently, customers were invited to throw one of the products affected and to contact their health care provider.
